4-P-Aminophenyl-1-Boc-Piperidine, with the CAS number 170011-57-1, is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group in organic synthesis, particularly for amines, indicating that the compound has a protected amine functionality. The presence of the para-aminophenyl group suggests that it has an aromatic character, which can influence its reactivity and interactions in various chemical environments. This compound is typically used in medicinal chemistry and organic synthesis, often as an intermediate in the development of pharmaceuticals. Its solubility, stability, and reactivity can vary depending on the solvent and conditions used in reactions. Additionally, the presence of both the aromatic and aliphatic components in its structure may contribute to its biological activity, making it a subject of interest in drug design and development. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

4-P-Aminophenyl-1-Boc-Piperidine

170011-57-1: 1-N-Boc-(4-aminophenyl)piperidine, Tert-Butyl 4-(4-Aminophenyl)Piperidine-1-Carboxylate, 4-(4-Amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

tert-butyl 4-(4-aminophenyl)piperidine-1-carboxylate

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CAS 170011-57-1: 4-P-Aminophenyl-1-Boc-Piperidine

tert-butyl 4-(4-aminophenyl)piperidine-1-carboxylate

Ref: IN-DA00393F

1-Boc-4-(4-aminophenyl)piperidine

Ref: 3D-FB51224

tert-Butyl 4-(4-Aminophenyl)piperidine-1-carboxylate

Ref: 3B-B5832

4-p-Aminophenyl-1-Boc-piperidine

Ref: 10-F036782

1-Boc-4-(4-aminophenyl)-piperidine

Ref: 54-OR322231